Wang H J, Chen T M, Cheng T Y
Plastic and Reconstructive Surgery and Burn Center, Department of Surgery, Tri-service General Hospital, Taipei, Taiwan, Republic of China.
J Trauma. 1997 Feb;42(2):177-82. doi: 10.1097/00005373-199702000-00002.
To answer the question whether a xenograft dermal substitute could enhance skin grafting, we used porcine dermis as a template for a widely expanded mesh autologous split-thickness skin (ASTS) graft in a rat model. Four groups of rats had received widely expanded meshed skin autografts to cover an excised back wound. Group 1 had a bed of autologous dermis, group 2 had porcine xenograft dermis, group 3 had widely expanded meshed autograft alone, and group 4 had no graft with the wound healing by contraction alone. Wounds were studied by clinical inspection for texture and contraction, and by histologic and immunofluorescent techniques. At 2 weeks, there was acceptable ASTS graft take, and most of the wound healed completely by 3 weeks. The integrity of this complex skin graft was maintained for 4 months but wound contraction gradually decreased overall wound size. Size was maintained better in the ASTS-autodermis and ASTS-xenodermis groups at postgraft 4, 5, and 6 weeks when compared with the ASTS graft, and there was no difference between the ASTS-autodermis and ASTS-xenodermis groups. Thus both allodermis and xenodermis provided a similar template to enhance widely expanded mesh skin growth and delay wound contraction. The pathologic studies indicate that the xenodermis collagen was replaced either by fibrosis or by biodegradation to rat collagen. The immunofluorescent study also reflected that anti-porcine antibody activity was hugely diminished in the ASTS-xenodermis graft wound after long-term follow-up. In conclusion, either autodermis or xenodermis enhances widely expanded mesh ASTS survival in a rat model, and could significantly maintain the original wound size better than ASTS graft without a template. In a long-term follow-up study, the porcine dermis was replaced either by fibrosis or biodegradation to rat dermis.
为了回答异种移植真皮替代物是否能促进皮肤移植的问题,我们在大鼠模型中使用猪真皮作为广泛扩展的网状自体中厚皮片(ASTS)移植的模板。四组大鼠接受了广泛扩展的网状自体皮肤移植以覆盖切除的背部伤口。第1组有自体真皮床,第2组有猪异种移植真皮,第3组仅有广泛扩展的网状自体移植皮片,第4组未进行移植,伤口仅通过收缩愈合。通过临床检查观察伤口的质地和收缩情况,并采用组织学和免疫荧光技术进行研究。术后2周,ASTS移植皮片成活情况良好,大多数伤口在3周时完全愈合。这种复合皮肤移植的完整性维持了4个月,但伤口收缩逐渐减小了整体伤口大小。与ASTS移植组相比,ASTS - 自体真皮组和ASTS - 异种真皮组在移植后4、5和6周时伤口大小维持得更好,且ASTS - 自体真皮组和ASTS - 异种真皮组之间无差异。因此,同种异体真皮和异种真皮都提供了类似的模板,以促进广泛扩展的网状皮肤生长并延迟伤口收缩。病理研究表明,异种真皮胶原蛋白被纤维化或被降解为大鼠胶原蛋白。免疫荧光研究还表明,长期随访后,ASTS - 异种真皮移植伤口中的抗猪抗体活性大幅降低。总之,在大鼠模型中,自体真皮或异种真皮均可提高广泛扩展的网状ASTS的成活率,并且比无模板的ASTS移植能更好地显著维持原始伤口大小。在长期随访研究中,猪真皮被纤维化或生物降解为大鼠真皮。